Cautions; Notes - Sunoptic Surgical LED-4500 Manual Del Usuario

connection between the illuminator and the patient. Such connections present a
risk to patient safety.
Instruments and/or light guides should be clean and dry before being connected
•
to the illuminator.
DO NOT modify the equipment without authorization from the manufacturer.
•
The illuminator is provided non-sterile and is not intended to be sterilized.
•
Use only the power cord supplied with illuminator or medically approved power
•
cords.
This device meets CISPR 11 Class A limits and is suitable for use in a hospital
•
environment. Performance of this device may be affected in proximity of another
device and/or equipment capable of producing high levels of RF emissions. In the
event performance of this device is affected due to high levels of RF emissions,
relocation of the suspected device and/or equipment producing high levels of RF
emissions, or the headlight system may reduce or eliminate the problem.

2.2. Cautions

• Before each procedure, carefully check the illuminator for damage. DO NOT use
a damaged illuminator.
• The user should verify the light guide end tip and the active illumination port are
of the same type before insertion. DO NOT attempt to force an end tip into an
incorrect port.
Only FUSED, end tip light guides manufactured by Sunoptic Technologies should
•
be used with the illuminator.
All servicing and repair must be performed by the manufacturer or qualified
•
service technicians.
Ensure that the air vents located on the illuminator are not obstructed to allow the
•
device to receive the necessary cooling to prevent an overheating.

2.3. Notes

If there is a power interruption during use, the illuminator will shut down and
•
automatically restart if the power switch remains in the ON position. There may
be a short delay as the unit reboots.
LIT-258 Sunoptic Surgical
Rev. A
®
Page 5 of 130
(English)